Senior SAS Programmer - Clinical Trials Lead (Remote)

Cytel; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading biostatistical consulting firm is seeking a Senior Statistical Programmer in the United Kingdom to support global pharmaceutical clients. The role involves advanced SAS programming, working on Phase I-IV clinical trials with responsibilities such as data manipulation, ad-hoc reporting, and adherence to CDISC standards. Candidates should have a Bachelor's degree and at least 8 years of experience in the pharmaceutical industry. The position is fully remote, offering a chance to contribute to innovative patient treatment programs.

Qualifications

• At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry.
• Solid experience in implementing CDISC SDTM / ADaM standards.
• Experience in leading projects with strong management skills.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Generate and validate SDTM and ADaM datasets.
• Create and review submission documents and communicate with internal teams.

Skills

SAS programming

Data manipulation

Clinical trial data analysis

CDISC SDTM/ADaM standards

QC/validation skills

Efficacy analysis proficiency

Ad-hoc reporting skills

Analytical skills

Troubleshooting skills

Education

Bachelor’s degree in Statistics, Computer Science, Mathematics

Job description

A leading biostatistical consulting firm is seeking a Senior Statistical Programmer in the United Kingdom to support global pharmaceutical clients. The role involves advanced SAS programming, working on Phase I-IV clinical trials with responsibilities such as data manipulation, ad-hoc reporting, and adherence to CDISC standards. Candidates should have a Bachelor's degree and at least 8 years of experience in the pharmaceutical industry. The position is fully remote, offering a chance to contribute to innovative patient treatment programs.